DHX30

DExH-box helicase 30 Q7L2E3 DHX30_HUMAN
Protein Coding Chr 3 3p21.31 Swiss-Prot reviewed Entrez 22907
Mutations
2,584
CL 265 · Tissue 2,264
Samples
523
CL 82 · Tissue 426
Peptides
448
unique mutant peptides
Transcripts
5
isoforms mutated

Stats by Source

Total, split by cell line (COSMIC CL / DepMap / PubMed) vs tissue (COSMIC primary tissue)

How the counts split by source
Stats by Source

Total = all mutations for this gene across every source.

Cell line = COSMIC Cell Lines Project + DepMap + PubMed.

Tissue = COSMIC primary-tissue (patient tumour) samples.

Total can exceed cell line + tissue: COSMIC tissue-derived models sit only in global, and a peptide can be shared across both.

TotalCell lineTissue
Mutations2,5842652,264
Samples52382426
Peptides44870377

Function

DHX30 · DExH-box helicase 30

DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this DEAD box protein family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. The family member encoded by this gene is a mitochondrial nucleoid protein that associates with mitochondrial DNA. It has also been identified as a component of a transcriptional repressor complex that functions in retinal development, and it is required to optimize the function of the zinc-finger antiviral protein. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Feb 2013].

Isoforms & Proteins

5 transcripts · UniProt mapping is sequence-verified (AA-safe)

About the isoform mapping
Isoforms & Proteins

Each Ensembl transcript (ENST) this gene is mutated on, with its matched UniProt accession.

The mapping is sequence-verified: the UniProt sequence is identical to the transcript translation, so amino-acid positions line up exactly. A * marks an unreviewed (TrEMBL) entry.

Counts are mutations and unique mutant peptides on each transcript.

TranscriptUniProtMutationsPeptides
ENST00000445061 Q7L2E3 586 423
ENST00000446256 Q7L2E3 516 391
ENST00000457607 Q7L2E3-2 496 374
ENST00000348968 H7BXY3* 494 375
ENST00000619982 Q7L2E3-3 492 372

Gene Properties

Type
Protein Coding
Chromosome
3
Cytoband
3p21.31
Entrez ID
Aliases
DDX30NEDMIALRETCOR

Recurrent Mutations

All 423 amino-acid changes on canonical ENST00000445061 · needle height = samples · drag the mini-map to zoom

What this lollipop shows
Recurrent Mutations

A lollipop / needle plot – the standard way to show recurrent mutations along a protein (as used by cBioPortal and MutationMapper).

X-axis = amino-acid position in the protein.

Needle height & head size = how often that exact amino-acid change was observed (its recurrence). Tall/large heads are mutational hotspots.

The most recurrent changes are labelled; hover any needle for the change, position and counts.

Mutation frequency across cancer types

% of samples with a missense/complex mutation in DHX30 · cell line vs tissue

How this frequency is counted
Cancer-type mutation frequency

For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in DHX30 – counted as distinct samples (a sample counts once no matter how many mutations it has).

Split into cell line and tissue; each cell shows mutated / total and the percentage. Cohorts with <20 samples are omitted. Ordered by combined frequency.

Cancer typeCell linesTissue samples
T-Lymphoblastic Leukemia
9/40 22%
0/0 0%
Endometrial Carcinoma
5/42 12%
30/612 5%
Colorectal Carcinoma
21/143 15%
92/3239 3%
Gastric Carcinoma
2/74 3%
40/1809 2%
Bladder Carcinoma
2/58 3%
19/956 2%
Cervical Carcinoma
2/35 6%
7/422 2%
Mesothelioma
2/62 3%
2/165 1%
Melanoma
6/210 3%
30/1899 2%
Hodgkins Lymphoma
0/16 0%
2/122 2%
Non-Small Cell Lung Carcinoma
7/304 2%
17/1390 1%
Ovarian Carcinoma
3/109 3%
8/998 1%
Other Solid Cancers
1/94 1%
15/1515 1%
Rhabdomyosarcoma
1/33 3%
1/171 1%
Non-Cancerous
0/104 0%
9/830 1%
Pancreatic Carcinoma
0/89 0%
16/1611 1%
Glioma
0/52 0%
20/2127 1%
Hepatocellular Carcinoma
1/46 2%
19/2210 1%
Head and Neck Carcinoma
1/85 1%
13/1574 1%
Squamous Cell Lung Carcinoma
0/57 0%
7/810 1%
Other Sarcomas
0/69 0%
6/699 1%
Prostate Carcinoma
5/13 38%
11/2105 1%
Breast Carcinoma
4/144 3%
20/3264 1%
Neuroendocrine Tumour
2/154 1%
3/577 1%
Kidney Carcinoma
3/85 4%
9/1862 0%
Thyroid Gland Carcinoma
2/45 4%
7/1592 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Biliary Tract Carcinoma
0/54 0%
5/950 1%
Osteosarcoma
0/45 0%
1/166 1%
Medulloblastoma
0/0 0%
2/450 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
11/2550 0%

Mutation Distribution

Where DHX30 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in DHX30 were found in each tissue, across the whole database.

Each bar is a tissue (cell-line and tissue names are merged to the standard tissue), split into cell line and tissue (patient tumour) contributions.

This shows the cancer-context where this gene is recurrently altered.

GTEx Expression

Median TPM across 54 healthy tissues

GTEx Portal ↗
About the expression data
GTEx Expression

Median gene expression (TPM) in normal, non-cancer human tissues from the GTEx project.

Useful for judging tumour specificity – a strong neoantigen target ideally comes from a gene with low expression in healthy tissues.

Scroll or drag the mini-axis below the chart to browse all tissues.

Mutations

All 2,584 mutations in DHX30

About the mutation list
Mutations

Every mutation record for this gene, across all samples and sources.

The Sample column links to the cell line (cell-line samples) or the tissue type (tissue samples).

Use the Type / Source filters, the search box, and column sorting to explore; each CAN-IMMUNE ID opens the full mutation & peptide view.

IDSampleTranscriptAA Change CDSTypeSourceMutant PeptideWild-type Peptide